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CS-W001157 4
Total: USD 88.00

7-Bromobenzofuran-3(2H)-one

  • CAS No. 519018-52-1

  • Cat. No. CS-W022534
  • Purity≥95%
  • MDL No.MFCD03160589

*For research and further manufacturing use only, not for direct human use.

7-Bromobenzofuran-3(2H)-one|CS-W022534

Structure of 519018-52-1

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General Information

  • CAS No. 519018-52-1
  • Cat. No. CS-W022534
  • Purity ≥95%
  • MDL No. MFCD03160589
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₈H₅BrO₂
  • Molecular Weight 213.03
  • Synonym(s) 7-Bromo-3-benzofuranone
  • SMILES O=C1COC2=C(Br)C=CC=C12

Description

7-Bromobenzofuran-3(2H)-one features a brominated benzofuran core with a ketone at the 3-position, delivering a rigid, electron-deficient scaffold ideal for transition metal-catalyzed coupling reactions. This bench-stable heterocycle integrates readily into complex molecular architectures, offering high functional group tolerance and predictable reactivity in medicinal chemistry and materials synthesis workflows.

Application

7-Bromobenzofuran-3(2H)-one serves as a versatile building block for the synthesis of biologically active heterocycles and pharmaceutical intermediates. Its bromine substituent enables facile palladium-catalyzed cross-coupling reactions, while the lactone functionality offers stability and compatibility with standard functional group manipulations. The compound exhibits excellent bench stability and is readily purified by recrystallization, facilitating its use in multi-step synthetic sequences.

Safety Information

Download SDS
GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H315-H319-H335
Precautionary Statements : P260-P261-P264-P270-P271-P280-P301+P310-P302+P352-P304+P340-P304+P341-P305+P351+P338-P312-P330-P332+P313-P337+P313-P362+P364-P363-P403+P233-P405-P501

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Computational Chemistry Data

  • TPSA   26.3
  • LogP   2.0242
  • H_Acceptors   2
  • H_Donors   0
  • Rotatable_Bonds   0

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